Azaarenes: 13 Rings in a Row by Cyclopentannulation
Steffen Maier, Nikolai Hippchen, Fabian Jester, Marcus Dodds, Michel Weber, Leon Skarjan, Frank Röminger, Jan Freudenberg, Uwe H. F. Bunz
Abstract
Cyclopentannulation was explored as a strategy to access large, stable azaarenes. Buchwald-Hartwig coupling of previously reported di- and tetrabrominated cyclopentannulated N,N'-dihydrotetraazapentacenes furnished stable azaarenes with up to 13 six-membered rings in a row and a length of 3.1 nm. Their optoelectronic and semi-conducting properties as well as their aromaticity were investigated.
Topics & Concepts
AromaticityCoupling (piping)ChemistryCrystallographyMaterials scienceOrganic chemistryMoleculeComposite materialSynthesis and Properties of Aromatic CompoundsOrganic Electronics and PhotovoltaicsN-Heterocyclic Carbenes in Organic and Inorganic Chemistry